Validation and assessment of variant calling pipelines for next-generation sequencing

Human genomics

Volumn 8, Issue , 2014, Pages 14-

  Pirooznia, Mehdi ^a   Kramer, Melissa ^a   Parla, Jennifer ^a   Goes, Fernando S ^a   Potash, James B ^a   McCombie, W Richard ^a   Zandi, Peter P ^b  

^a Johns Hopkins University ^*

^b JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BIPOLAR DISORDER; COMPUTER PROGRAM; DNA SEQUENCE; EXOME; GENETICS; HIGH THROUGHPUT SEQUENCING; HUMAN; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL ANALYSIS; VALIDATION STUDY;

BIPOLAR DISORDER; DATA INTERPRETATION, STATISTICAL; EXOME; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA; SOFTWARE;

EID: 84907687102     PISSN: None     EISSN: 14797364     Source Type: Journal    
DOI: 10.1186/1479-7364-8-14     Document Type: Article

References (0)